My fiance just released an album dedicated to his mother who has MS. Half of the proceeds will go straight to the MS society. Support good music for a great cause! Please!
be ready to fight and make a huge stock of sense of humor and sarcasm, it will be easier. important not to lose heart, as long as we think we can be alive
Help Jeff Johnson raise money for research to find a cure for Multiple Sclerosis. Visit his fundraising home page at nationalMSsociety home page and add to the URL /goto/jeffjohnson
In an ideal world, the ability of the medical system to use immunosuppressive drugs to target the entire destructive reaction occurs;but ,although this animation shows how wonderfully complex the cytokines, substance p, TNFalpha's, etc. are in the body, blue lights (steroids, immunosuppressives) are not the end all/ be all for therapy. Improving the system that had the breakdown in the first place is more useful. Supporting the body, nervous system, (can you say psychoneuroimmunology?)is best.
I was recently diagnosed with MS November 16, 2011 and I'm only 21 and it just feels like my life was starting and now taking a toll out of control. But I really liked this video, I sat here and cried.
@cupcakeezombiee I cried at watching this video too. I was diagnosed with MS on August 2009 and I am now 36 years old. I still feel like my life is a little out of control, but things have been getting better. You are not alone
Wake up, people! Yes, it's very depressing, yes MS is giving us a hell of a time, but if you'll put your hands down, it will destroy you! My country doesn't care about people with MS (because there are a couple of hundreds), but I did all I could and got "The Liberation Treatment" done! I had Relapsing Remitting MS which got into Secondary Progressive MS, but this procedure helped stop the progression and more important, now I can walk normally!
Could not have done this better...MS is so confusing, unpredictable...your video was just on point. You are brave I pray you have success on this journey. dx- July 2004
Just wanted to update from message below, written on day of receipt of THE letter. I am facing this, I am strong, I am carrying on with my plans, I'm still making dances for my Zumba classes in Sweden where I have recently moved. I will continue dancing for as long as I can move, however, I can move. It's what keeps me alive.
I am a Dance Artist.. I have had bouts of unexplained numbness down my right side, creepy body sensations, pins and needles in my feet, numb hands and finger tips for over a year.
I opened a letter yesterday saying that The MRI I had is compatible with Demyelination and in view of my symtoms it 'suggests' MS.
My first thought was great at least I know what it is wrong with my body now. I'm not making it up, I'm not going mad, There is a reason for these feelings.
Amazing I never cry at anything I thought that my crying abilities were broken coming back from combat and finding out I had Cadasil which is a form of MS I cried till i could not cry any longer. This video shows how some of us can and may feel having this disease. I felt like my heart was grabbed and squeezed till I cried again. Thank you for this Celitan7. Bravo!!!
There is now a Reformed Multiple Sclerosis Society that is urging for the medical community to check out Dr Paolo Zamboni's discovery that MS is caused by poor blood drainage from the brain. The answer to restore this blood drainage from the brain is angioplasty. Watch the before & afters for this surgery called CCSVI on youtube- simply amazing. In just 24 hours a world of difference. Standing on one foot eyes closed in just 24 hours!
Tears ran down my cheeks...This is exactly how I experience my own MS to. The picture with "pain"; I do that a lot....Shared it with my family and I think that they understand things a little better no. Sometimes it can be simpler to understand when its someone you dont have a personal relation to who speaks or by music. If you know how i mean....All my love!
@CeliTan7 ...this is really "helping"... First of all, USA at least gives MS patients some drugs to help stop the progression (my country doesn't do anything)
Second, now you can do "The Liberation procedure"! And, as I know, it is covered by your health insurance!
Here are some links, so you can learn more about the procedure.
/watch?v=C_RXs5dPh6E
/watch?v=y9fn3tbDj1s
(I have Secondary Progressive form of MS and it helped! Now I can walk a lot better!)
CCSVI Clinic Receives Joint IRB Approval for Aftercare Protocol Study.
The joint application between Noble Hospital and CCSVI Clinic has been approved through the IEC Institutional Review Board (IRB) that will allow researchers to use patient data to study their new extended and enhanced aftercare treatment protocol. Please Call 888-419-6855 to know more about participating in the study. Log on to ccsviclinic. ca for more information. Email apply -at- ccsviclinic. ca
Thank you for making the video. ;)
Atiram77 2 days ago
How do I give this a "thumbs up"? Great work though. :)
jmacman007 1 month ago
This has been flagged as spam show
My fiance just released an album dedicated to his mother who has MS. Half of the proceeds will go straight to the MS society. Support good music for a great cause! Please!
itunes.apple.com/us/album/jnewryep/id476015357
Blessings
JessicaSunshineMusic 1 month ago
I was dńx w/MS on 6/1997. It's been 15 years living with my MS. Staying positive and taking care of myself using Rebif
Dalicea97 1 month ago 2
Been diagnosed 2 and a half years ago, living normally but scared. And I'm 21.
Wish you all the best. Hugs from Croatia. :)
traxdata666 1 month ago
been diagnosed 3 years ago,living a normal life tough symptoms sometimes are very bad,very touching video.we will survive. "just keep walking"
souheilabd 1 month ago
be ready to fight and make a huge stock of sense of humor and sarcasm, it will be easier. important not to lose heart, as long as we think we can be alive
thanks for the video
penguinet75 1 month ago in playlist More videos from CeliTan7
thank you for this video ! allt he best to you
heidibjorg 1 month ago
Help Jeff Johnson raise money for research to find a cure for Multiple Sclerosis. Visit his fundraising home page at nationalMSsociety home page and add to the URL /goto/jeffjohnson
Ekorn999 3 months ago
In an ideal world, the ability of the medical system to use immunosuppressive drugs to target the entire destructive reaction occurs;but ,although this animation shows how wonderfully complex the cytokines, substance p, TNFalpha's, etc. are in the body, blue lights (steroids, immunosuppressives) are not the end all/ be all for therapy. Improving the system that had the breakdown in the first place is more useful. Supporting the body, nervous system, (can you say psychoneuroimmunology?)is best.
arkmoblvet1998 3 months ago
Comment removed
arkmoblvet1998 3 months ago
I was recently diagnosed with MS November 16, 2011 and I'm only 21 and it just feels like my life was starting and now taking a toll out of control. But I really liked this video, I sat here and cried.
cupcakeezombiee 3 months ago
@cupcakeezombiee I cried at watching this video too. I was diagnosed with MS on August 2009 and I am now 36 years old. I still feel like my life is a little out of control, but things have been getting better. You are not alone
Ladyred0097 2 months ago
You don't have MS.
Your doctors and brain are telling you that you have it but you don't
You have mercury + other heavy metals in your body.
EVERYONE DOES. It's in our food, land air, ect.
Get a full heavy metal test @ a wellness centre and you will be SHOCKED at the results as heavy metals are causing your symptoms.
Why do you think I would take so much time out of my life to help people?
Because, I care and I know I can help you.
Just go and get it done? It's so simple!
vancouverislandbass 3 months ago
Wake up, people! Yes, it's very depressing, yes MS is giving us a hell of a time, but if you'll put your hands down, it will destroy you! My country doesn't care about people with MS (because there are a couple of hundreds), but I did all I could and got "The Liberation Treatment" done! I had Relapsing Remitting MS which got into Secondary Progressive MS, but this procedure helped stop the progression and more important, now I can walk normally!
/watch?v=C_RXs5dPh6E
/watch?v=y9fn3tbDj1s
AlexLopatenco 4 months ago
Could not have done this better...MS is so confusing, unpredictable...your video was just on point. You are brave I pray you have success on this journey. dx- July 2004
jaybella1986 4 months ago
Just wanted to update from message below, written on day of receipt of THE letter. I am facing this, I am strong, I am carrying on with my plans, I'm still making dances for my Zumba classes in Sweden where I have recently moved. I will continue dancing for as long as I can move, however, I can move. It's what keeps me alive.
MsCSimmonds 4 months ago in playlist MS
I am a Dance Artist.. I have had bouts of unexplained numbness down my right side, creepy body sensations, pins and needles in my feet, numb hands and finger tips for over a year.
I opened a letter yesterday saying that The MRI I had is compatible with Demyelination and in view of my symtoms it 'suggests' MS.
My first thought was great at least I know what it is wrong with my body now. I'm not making it up, I'm not going mad, There is a reason for these feelings.
Movement is me-What Now?
MsCSimmonds 5 months ago
wow!! brightin my day.. 03:21-03:25
thallious9876 5 months ago
I HAVE MS TOO . SMOKING WEED HELPS ALOT WITH SEIZURES N DEPRESSION . THE ONLY TIME I GET DEPRESSED NOW IS WHEN I RUN OUT . ;/
jessemac13 6 months ago
Amazing I never cry at anything I thought that my crying abilities were broken coming back from combat and finding out I had Cadasil which is a form of MS I cried till i could not cry any longer. This video shows how some of us can and may feel having this disease. I felt like my heart was grabbed and squeezed till I cried again. Thank you for this Celitan7. Bravo!!!
HAAKONAS 6 months ago
This has been flagged as spam show
There is now a Reformed Multiple Sclerosis Society that is urging for the medical community to check out Dr Paolo Zamboni's discovery that MS is caused by poor blood drainage from the brain. The answer to restore this blood drainage from the brain is angioplasty. Watch the before & afters for this surgery called CCSVI on youtube- simply amazing. In just 24 hours a world of difference. Standing on one foot eyes closed in just 24 hours!
2ndSamuel710 6 months ago
Love your video! I have MS too and I can relate to the things your video was portraying.
Godivahair 6 months ago
This has been flagged as spam show
Tears ran down my cheeks...This is exactly how I experience my own MS to. The picture with "pain"; I do that a lot....Shared it with my family and I think that they understand things a little better no. Sometimes it can be simpler to understand when its someone you dont have a personal relation to who speaks or by music. If you know how i mean....All my love!
TheVompan 6 months ago
Comment removed
TheVompan 6 months ago
Ah, thank you so much. I'm glad you liked it.
CeliTan7 7 months ago
@CeliTan7 ...this is really "helping"... First of all, USA at least gives MS patients some drugs to help stop the progression (my country doesn't do anything)
Second, now you can do "The Liberation procedure"! And, as I know, it is covered by your health insurance!
Here are some links, so you can learn more about the procedure.
/watch?v=C_RXs5dPh6E
/watch?v=y9fn3tbDj1s
(I have Secondary Progressive form of MS and it helped! Now I can walk a lot better!)
AlexLopatenco 4 months ago
GREAT JOB!!!! I LOVE IT!!! Thank you so much, Anastacia. Fighting the fight w/you!!!
crdefhead 7 months ago
This has been flagged as spam show
CCSVI Clinic Receives Joint IRB Approval for Aftercare Protocol Study.
The joint application between Noble Hospital and CCSVI Clinic has been approved through the IEC Institutional Review Board (IRB) that will allow researchers to use patient data to study their new extended and enhanced aftercare treatment protocol. Please Call 888-419-6855 to know more about participating in the study. Log on to ccsviclinic. ca for more information. Email apply -at- ccsviclinic. ca
Gregmills007 11 months ago
Thank you, Anastacia. From a fellow fighter.
savnsan 11 months ago
PS song title and artist please.
Many thanks in advance.
mooseasaurusrex 1 year ago
@mooseasaurusrex The song title, and artist are in the credits at the end.
CeliTan7 11 months ago
I was looking for a good fight.
And then MS showed up.
I am now the MonSter it fears. `;}>
mooseasaurusrex 1 year ago
Has anyone tried upper cervical care, from a chiropractor? I have read about the studies they found with sufferers of M.S.
The outcome has shown to be pretty amazing.
Share the hope.
CeliTan7 1 year ago